X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (5373) 5373
Publication (413) 413
Newspaper Article (352) 352
Newsletter (181) 181
Magazine Article (42) 42
Book Chapter (31) 31
Book Review (31) 31
Web Resource (16) 16
Book / eBook (15) 15
Reference (14) 14
Dissertation (11) 11
Conference Proceeding (9) 9
Data Set (2) 2
Streaming Video (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (3681) 3681
dwarfism (2610) 2610
female (2573) 2573
male (2517) 2517
dwarfism - genetics (2100) 2100
index medicus (1417) 1417
child (1296) 1296
animals (1199) 1199
genetics & heredity (1075) 1075
mutation (1031) 1031
syndrome (895) 895
child, preschool (886) 886
adult (884) 884
adolescent (838) 838
infant (662) 662
endocrinology & metabolism (645) 645
phenotype (644) 644
mice (634) 634
genetic aspects (632) 632
pedigree (567) 567
radiography (550) 550
infant, newborn (534) 534
research (515) 515
abnormalities, multiple - genetics (499) 499
pediatrics (478) 478
growth (412) 412
gene (406) 406
genes (390) 390
dwarfism - diagnosis (376) 376
dwarfism - pathology (365) 365
dwarfism, pituitary - genetics (365) 365
analysis (354) 354
genetics (337) 337
pregnancy (325) 325
mutations (324) 324
genes, recessive (307) 307
osteochondrodysplasias - genetics (307) 307
expression (304) 304
short stature (291) 291
dwarfism - diagnostic imaging (279) 279
intellectual disability - genetics (271) 271
gene expression (266) 266
research article (265) 265
proteins (259) 259
dwarfism - complications (256) 256
cell biology (252) 252
molecular sequence data (252) 252
biochemistry & molecular biology (251) 251
dwarfism - metabolism (249) 249
physiological aspects (247) 247
diagnosis, differential (245) 245
children (243) 243
base sequence (237) 237
dysplasia (236) 236
growth hormone (234) 234
consanguinity (231) 231
middle aged (230) 230
genetic research (224) 224
achondroplasia (214) 214
medicine (211) 211
dwarfism - physiopathology (206) 206
microcephaly - genetics (206) 206
multidisciplinary sciences (203) 203
somatotropin (196) 196
growth disorders - genetics (192) 192
bone diseases, developmental - genetics (188) 188
genetic disorders (188) 188
growth hormone - deficiency (188) 188
rats (187) 187
genotype (182) 182
amino acid sequence (179) 179
body height (176) 176
gene mutations (176) 176
article (175) 175
diagnosis (174) 174
plant sciences (173) 173
health aspects (165) 165
chromosome disorders (164) 164
face - abnormalities (164) 164
receptors, somatotropin - genetics (163) 163
heterozygote (161) 161
life sciences (160) 160
homozygote (154) 154
biology (147) 147
insulin-like growth factor i - metabolism (147) 147
signal transduction (147) 147
skeletal dysplasia (146) 146
dwarfism - etiology (144) 144
dna mutational analysis (143) 143
deficiency (141) 141
genomes (141) 141
disease (139) 139
karyotyping (138) 138
dwarfism, pituitary - drug therapy (137) 137
bone and bones - abnormalities (135) 135
cells, cultured (135) 135
chromosome aberrations (135) 135
science (135) 135
polymerase chain reaction (134) 134
mice, mutant strains (133) 133
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (7) 7
Robarts - Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Gerstein Science - Theses (1) 1
OISE - Children's Literature (1) 1
Scarborough Hospital - General (1) 1
UofT Schools - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (5472) 5472
French (160) 160
German (141) 141
Spanish (54) 54
Japanese (52) 52
Italian (46) 46
Russian (18) 18
Chinese (15) 15
Polish (14) 14
Portuguese (10) 10
Finnish (8) 8
Turkish (7) 7
Dutch (6) 6
Romanian (6) 6
Czech (4) 4
Slovak (4) 4
Danish (3) 3
Hungarian (3) 3
Korean (2) 2
Norwegian (2) 2
Hebrew (1) 1
Lithuanian (1) 1
Persian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 01/2018, Volume 102, Issue 1, pp. 27 - 43
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 11/2012, Volume 8, Issue 11, p. e1002945
A homozygous mutational change in the Ataxia-Telangiectasia and RAD3 related (ATR) gene was previously reported in two related families displaying Seckel... 
H2AX | PRIMORDIAL DWARFISM | PHOSPHORYLATION | DNA-DAMAGE RESPONSE | ORIGIN RECOGNITION COMPLEX | II MOPD-II | GENETICS & HEREDITY | STRESS | MEIER-GORLIN SYNDROME | LOCUS | SSDNA | Osteochondrodysplasias - pathology | Microcephaly - genetics | Growth Disorders - pathology | Humans | Fetal Growth Retardation - genetics | Male | Micrognathism - pathology | DNA-Binding Proteins - deficiency | DNA-Binding Proteins - metabolism | RNA Splicing | Osteochondrodysplasias - genetics | Microcephaly - pathology | Patella - abnormalities | Cell Cycle Proteins - genetics | Female | Dwarfism - pathology | Protein-Serine-Threonine Kinases - metabolism | Congenital Microtia | Ear - abnormalities | Micrognathism - genetics | Cell Cycle Proteins - metabolism | Gene Expression Regulation | Protein-Serine-Threonine Kinases - genetics | Signal Transduction - genetics | Ataxia Telangiectasia Mutated Proteins | Codon, Nonsense | DNA-Binding Proteins - genetics | Fetal Growth Retardation - pathology | Patella - pathology | Dwarfism - genetics | Adaptor Proteins, Signal Transducing - deficiency | Adaptor Proteins, Signal Transducing - genetics | Heterozygote | Ear - pathology | Adaptor Proteins, Signal Transducing - metabolism | Growth Disorders - genetics | Gene mutations | Seckel syndrome | Physiological aspects | Development and progression | Ataxia telangiectasia | Genetic aspects | Research | Science | Medical research | Mutation | Genes
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2015, Volume 96, Issue 4, pp. 612 - 622
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 2, p. e14726
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2011, Volume 43, Issue 4, pp. 350 - 356
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 02/2016, Volume 25, Issue 3, pp. 472 - 483
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2011, Volume 6, Issue 11, p. e28069
Background: Plant cytochromes P450 are involved in a wide range of biosynthetic reactions and play various roles in plant development. However, little is known... 
ENCODES | ARABIDOPSIS-THALIANA | CELL ELONGATION | ACID OMEGA-HYDROXYLASE | ENZYME | GENE | GIBBERELLIN | BIOLOGY | FUNCTIONAL-ANALYSIS | DELLA PROTEIN SLR1 | RICE | Cytochrome P-450 Enzyme System - metabolism | Gene Expression Profiling | RNA, Messenger - metabolism | Genetic Complementation Test | Oryza - anatomy & histology | Schizosaccharomyces - genetics | Oryza - genetics | RNA Interference | Fertility | Germination - genetics | Plants, Genetically Modified | DNA Transposable Elements - genetics | Gene Expression Regulation, Plant | Plant Proteins - metabolism | Multigene Family - genetics | Pollen - growth & development | Gene Dosage - genetics | Genome, Plant - genetics | RNA, Messenger - genetics | Organ Size | Lipid Metabolism | Mutation - genetics | Oryza - enzymology | Mutagenesis, Insertional - genetics | Arabidopsis - genetics | Gene Expression Regulation, Enzymologic | Plant Proteins - genetics | Phenotype | Cytochrome P-450 Enzyme System - genetics | Plant Leaves - anatomy & histology | Schizosaccharomyces - cytology | Chromosome Segregation - genetics | Production management | Genetically modified plants | Transposons | RNA | Gibberellins | Germination | Physiological aspects | Genetic engineering | Rice | Cytochrome | Transcription | Laboratories | Genomics | Biosynthesis | Dosage | Transgenic plants | Defects | Dwarfism | Proteins | Life sciences | Pollen | Lipid metabolism | Elongation | Cytochromes P450 | Plants (botany) | RNA-mediated interference | Cytochrome P450 | Double-stranded RNA | Cell division | Metabolism | Gene expression | Transposase | Fatty acids | Ribonucleic acids | Cytochromes | Mutation | Biosensors
Journal Article